1 |
Beech and F5H-poplar lignin under formaldehyde stabilization;
lignin solution 20 mL |
5 wt% Ru/C; 100 mg cat. |
THF |
250 °C, H2 4 MPa, 15 h |
47% Phenolic monomers for beech
lignin and 78% for F5H-poplar
lignin |
4-n-Propylsyringol and 4-n-propanolsyringol |
(605) |
2 |
Birch spruce and F5H-poplar
lignin extracted with acetaldehyde
(AA) and propionaldehyde (PPA) protection; lignin solution 20 mL |
Pd/C; 250 mg Ru/C; 100 mg Ni/C; 100 mg |
1,4-dioxane |
200 °C, H2 4 MPa, 20 h |
48% Phenolic monomers for birch lignin, 70% for F5H-poplar
lignin, and 20% from spruce lignin; the yields listed here are based
on Pd/C |
High selectivity (80%) to 4-n-propanolsyringol
for poplar lignin |
(648) |
3 |
Endocarp lignin under propanal-assisted
fractionation; 100
mg |
Ru/C; 1:1 |
THF |
250 °C,
H2 4 MPa, 3 h |
Up to 120 g monomers/kg biomass |
Ca. 75% selectivity
to propylguaiacol/syringol |
(649) |
4 |
Propylidene acetal-stabilized
lignin from birch, 2.5mg/mL in
1,4-dioxane/methanol mixture |
Ni/C, Ru/C |
1,4-dioxane/methanol (2:8, v/v) |
180 °C, H2 6 MPa, 20 h; flow reactor: lignin,
feed: 0.1mL/min, lignin solution, flow rate of H2: 50 mL/min |
45% Phenolic monomers over Ni/C and 40% phenolic monomers over Ru/C |
Approximately 39% 4-n-propylsyringol
over Ni/C and approximately 15–20%
4-n-propylsyringol over Ru/C |
(650) |
5 |
Ethyl glycol-incorporated lignin (α-alkoxylated
lignin);
200 mg |
Ru/C; 1:1 |
MeOH |
220
°C, H2 4 MPa, 18 h |
24% Monophenolic monomers |
49% Selectivity to
4-n-propylsyringol |
(654) |
6 |
Catechyl lignin
from enzymatic hydrolysis (C-lignin) and C-lignin
containing biomass; 200 mg |
Pt/C, Pd/C, Ru/C; 0.5:1 |
MeOH, 1,4-dioxane, or THF |
200 °C, H2 4 MPa, 15 h |
Up to 85 mol% catechyl monomers with isolated C-lignin |
Approximately 60 mol% catechylpropane
with Pd/C; 55% mol catechylpropanol
with Ru/C |
(655) |
7 |
Isolated C-lignin by ChCl/LA; 50 mg |
Pd/C, Ru/C; 0.3:1 |
MeOH |
200 °C,
H2 3 MPa, 4 h |
Catechyl monomers in 29.6 wt% |
24 wt% Catechylpropanol with Pd/C |
(656) |
8 |
C-lignin
sample from endocarp of castor seed coats; coats extracted
by enzymatic and mild acidolysis treatment; 50 mg |
Ru/ZnO/C;
0.3:1 |
MeOH |
200 °C, H2 3
MPa, 4 h |
Catechyl monomers
in 66 mol% |
77% High selectivity
to propenylcatechol |
(657) |